Muscular dystrophy drug

ABSTRACT

The object of the present invention is to provide a drug having therapeutic effect on muscular dystrophy without lowering renal function. The therapeutic drug for muscular dystrophy of the present invention comprises a caldecrin or a caldecrin gene.

This application claims benefit of priority to Japanese patentapplication No. 2006-355346 filed on Dec. 28, 2006, and provisionalpatent application in the U.S. No. 60/929,034 filed on Jun. 8, 2007, thecontents of which are incorporated by reference herein.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a drug for treating muscular dystrophy.

2. Description of the Related Art

Main pathological changes by muscular dystrophy are degeneration andnecrosis of skeletal muscle. Clinically, muscular dystrophy is a geneticdisease accompanied with progressive loss of muscle strength.

As causes of muscular atrophy leading to a loss of muscle strength, anabnormality of in motor nerves in addition to an abnormality of muscleitself is exemplified. A muscular atrophy due to an abnormality ofmuscle itself is called as myogenic muscular atrophy, and a muscularatrophy due to an abnormality of motor nerves is called as neurogenicmuscular atrophy. In neurogenic muscular atrophy, no abnormality isfound in muscle but an abnormality appears in motor nerves and musclesmovement, leading to muscular atrophy. Muscular dystrophy is arepresentative disease of myogenic muscular atrophy.

Although the cause of muscular dystrophy is not quite clear,deficiencies and abnormalities in a series of proteins of dystrophinpresent just below a muscular plasma membrane, adhalin present in aplasma membrane, merosin present in a basement membrane and the like areconsidered as possible causes.

Based on such knowledge, it is considered as a possible treatment formuscular dystrophy to induce dystrophin and the like. However, theireffectiveness has not been confirmed in clinical trials.

As a therapeutic drug, a protein anabolic hormone, a growth hormone, acalcium antagonist, a protein-degrading enzyme inhibitor such asbestatin, a muscle relaxant such as sodium dantrolene and the like havebeen used so far. However, although these drugs exhibit a certain degreeof inhibiting effect on progression of symptoms at an initial period ofadministration, the effect does not last. Thus, in the presentsituation, rehabilitation and the like are mainly carried out as atreatment for preventing progression of dysfunction. Namely, the drugshaving a sufficient therapeutic effect on muscular dystrophy have notbeen known. Therefore, drugs for treating muscular dystrophy have beenstudied.

For example, it is described in TAKAOKA et al., Journal of Bone andMineral Metabolism, vol. 18, pp. 2-8 (2000), that a patient ofprogressive muscular dystrophy who had almost been immobilized for 4years was administered a crude extract derived from pig pancreas. As aresult, an improvement was seen in one week, and the patient could goback home in one month. It is further described in the document that amuscular dystrophy patient was administered the same crude extract, sothat the patient gained weight in 8 months and came to be able to raisethe leg high in 10 months.

However, precise experimental conditions are not described in the aboveacademic document at all, so the reliability of the results isquestionable. For example, it is unlikely that no other treatment wastaken at all while the crude extract was administered; therefore, thereis no certain evidence that the above improvement effects are resultedfrom the crude extract alone. In fact, although it is described in thedocument that the above crude extract has a strong activity for reducingBUN, i.e. serum urea nitrogen level, which is to be an indicator ofmuscular dystrophy, the effect was weak when the present inventorscarried out a similar experiment.

In the above academic document, it is also described that N-terminalamino acid sequence of the protein further purified from the crudeextract indicates high homology with human elastase IIIB. In addition,it is concluded that bone/calcium metabolism regulating activity of thecrude extract results from elastase IIIB.

However, the effects of human elastase IIIB on muscular dystrophy havenot been proved directly, and there is no report of its clinical use. Ofcourse, it has not been put to practical use.

Tomomura who is one of the inventors of the present invention isolatedcaldecrin from pig pancreas and found that the caldecrin reduces serumcalcium level (Japanese unexamined patent publication No. 4-279598).Further, Tomomura completed method of producing caldecrin using acaldecrin gene (Japanese unexamined patent publication No. 8-298990).However, the effects of the caldecrin on muscular dystrophy have neverreported so far.

BRIEF SUMMARY OF THE INVENTION

As described above, muscular dystrophy is an intractable diseaseaccompanied with a gradual loss of motor function, and its fundamentaltreatment method has not been established. Further, various studies havebeen carried out with respect to muscular dystrophy, but there is nodrug that has been put to practical use and exerts sufficient effect.

PX, which is a crude extract derived from pig pancreas, is reported inthe above academic document to have indicated marked effects on musculardystrophy, but has not been put to practical use. Though the reason isunknown, according to the experiment by the present inventors, PX doesnot have a markedly superior effect on reduction of BUN and PX has adefect of increasing creatinine level in blood. Creatinine is normallyexcreted directly into urine, but if there is an abnormality in renalfunction, it is accumulated in blood. Thus, creatinine is used as anevaluation index of renal functions. Namely, PX has a problem oflowering renal functions.

The problem to be solved by the present invention is to provide a drugwhich has a therapeutic effect on muscular dystrophy and does not lowerrenal functions.

The present inventors intensively studied for solving the above problem,and accomplished the present invention with a finding that caldecrin anda caldecrin gene show an excellent therapeutic effect on musculardystrophy without damaging renal functions.

A first muscular dystrophy drug of the present invention comprises acaldecrin.

A second muscular dystrophy drug of the present invention comprises afollowing protein (a) or a following protein (b):

(a) a protein having the amino acid sequence of SEQ ID No. 1 or SEQ IDNo. 2;(b) a protein formed by deletion, substitution and/or addition of one orseveral amino acids of a protein having amino acid sequence of SEQ IDNo. 1 or SEQ ID No. 2, and having therapeutic effect on musculardystrophy.

A third muscular dystrophy drug of the present invention comprises acaldecrin gene.

A vector of the present invention comprises the caldecrin gene.

A transformed cell of the present invention comprises the vector.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a diagram showing the change of serum urea nitrogen level whenhuman caldecrin or human caldecrin gene expression vector isadministered to a muscular dystrophy-affected model mouse.

FIG. 2 is photographs showing results of H. E. stain of muscular tissuein a normal mouse and a muscular dystrophy-affected model mouse to whichhuman caldecrin or human caldecrin gene expression vector wasadministered.

FIG. 3 is fluorescent microscope photographs by autonomous fluorescenceof Evans blue showing conditions of muscular tissues in a normal mouseand a muscular dystrophy-affected model mouse to which human caldecrinor human caldecrin gene expression vector was administered.

DETAILED DESCRIPTION OF THE INVENTION

The therapeutic drug for muscular dystrophy according to the presentinvention is characterized in comprising a caldecrin.

The caldecrin is discovered by Tomomura et al. The pro-type of thecaldecrin consists of 252 amino acids having a molecular weight of about28 kDa, and the prepro-type thereof consists of 268 amino acids having amolecular weight of about 30 kDa. In mouse, the caldecrindose-dependently lowers serum calcium concentration, and has aninhibitory activity against parathyroid hormone (PTH)-induced calciumrelease in embryonic bone cell culture system.

A type of the caldecrin used in the present invention is notparticularly limited as long as it has a therapeutic effect on musculardystrophy, and includes, for example, a caldecrin derived from human anda caldecrin derived from rat. Therapeutic effects of these caldecrins onmuscular dystrophy are demonstrated in the following Examples.

In the caldecrin of the present invention, a mature-type, a pro-type anda prepro-type thereof are included. Besides, a caldecrin bonded to alabel sequence or a marker group can also exert the same activity as thecaldecrin.

The caldecrin is homologous with serine protease such as elastase andchymotrypsin. For example, a gene coding pro-type rat caldecrin (SEQ IDNo.3) and a gene coding pro-type rat elastase IV (SEQ ID No.5) show highhomology. However, in comparison of both sequences, adenine is insertedat 243rd in pro-type rat caldecrin gene. The insertion causes frameshift mutation. In addition, cytosine is inserted at 312th in pro-typerat elastase IV gene. As a result, in comparison between pro-type ratcaldecrin (SEQ ID No.1) and pro-type rat elastase IV (SEQ ID No.6),amino acid sequences of both of the proteins are clearly different ataround a middle thereof (refer to SEQ ID No.1 and SEQ ID No.6).Specifically, while amino acid sequences of 1st to 80th and 105th orlater in pro-type rat caldecrin (SEQ ID No.1) and pro-type rat elastaseIV (SEQ ID No.6) are almost same, amino acid sequences of 81st to 104thin both of the amino acid sequences are different at all by theabove-mentioned insertion of adenine and cytosine, although the 81stamino acid in both of the amino acid sequences happens to be identifiedeach other as glutamic acid in spite of the frame shift mutation.

Further, the caldecrin has a common feature with elastase IIIB, which issaid to be an active component of the crude extract derived from pigpancreas, in that they have an effect of lowering serum calcium innormal mouse, but they are clearly different in their structures and theother effects.

For example, the caldecrin does not lose an effect on lowering serumcalcium in mouse and an inhibitory effect on PTH, even when treated withphenyl methane sulfonyl fluoride (PMSF) which is an irreversible serineprotease inhibitor. On the other hand, elastase IIIB loses an effect oflowering serum calcium and an inhibitory effect on PTH by PMSF.

Examples of the caldecrin used in the present invention may comprise thefollowing protein (a) or (b):

(a) a protein having amino acid sequence of SEQ ID No. 1 or SEQ ID No.2;(b) a protein formed by deletion, substitution and/or addition of one orseveral amino acids of a protein having amino acid sequence of SEQ IDNo.1 or SEQ ID No.2, and having therapeutic effect on musculardystrophy.

The caldecrins of SEQ ID No.1 and SEQ ID No.2 are pro-type containingpro-sequence consisting of 1st to 13th amino acids. Such a pro-typecaldecrin becomes a mature-type caldecrin by breakage of thepro-sequence by, for example, protease present in living body afteradministration. However, the 1st cysteine forms intramolecular disulfidebond with inside cysteine, and the pro-sequence is also bound in themature-type. Accordingly, such a mature-type is included in the protein(b), which is formed by bonding and breakage of the pro-sequence in theprotein (a).

The protein (b) of the present invention includes a prepro-typecaldecrin in which a pre-sequence is bound at N-terminal of the protein(a). The caldecrin is excreted as pro-type to the outside of a cell,after production inside of the cell as prepro-type and breakage of thepre-sequence. A pre-sequence of rat caldecrin is SEQ ID No.7, and apre-sequence of human caldecrin is SEQ ID No.8.

The caldecrin according to the present invention comprises a proteinformed by deletion, substitution and/or addition of one or several aminoacids of a protein having amino acid sequence of SEQ ID No.1 or SEQ IDNo.2, and having therapeutic effect on muscular dystrophy. For example,in order to enhance activity, stability or the like, the protein (b) maybe formed by adding an amino acid or a peptide to N-terminal orC-terminal of the protein (a). Preferably, such an amino acid or apeptide is added to N-terminal thereof.

The number of amino acids to be deleted, substituted or added ispreferably from 1 to 10, more preferably from 1 to 5, even morepreferably 1 to 2. The amino acid sequence of SEQ ID No.1 or SEQ ID No.2that has been deleted, substituted or added preferably has an identityof 80% or more with the amino acid sequence of the human caldecrin orthe rat caldecrin, more preferably has an identity of 90% or more, andeven more preferably an identity of 95% or more. The identity can bedetermined by a publicly known method using a software program such asBLAST (Basic Local Alignment Search Tool). The substituting amino acidspreferably belong to the same classification of the amino acid to besubstituted. Examples of such a classification include, in addition toclassification such as neutral amino acid, acidic amino acid and basicamino acid, classification such as aliphatic amino acid, imino acid, andaromatic amino acid, and further, classification such as branched aminoacid, hydroxy amino acid, sulfur-containing amino acid, and acid amideamino acid.

The term, “having a therapeutic effect on muscular dystrophy”, in thedefinition in the above protein (b) means that at least one of theeffects as a therapeutic agent for muscular dystrophy is equivalent orsuperior to that of a protein having an amino acid sequence of SEQ IDNo.1 or SEQ ID No.2. The effects of the therapeutic agent for musculardystrophy include, in addition to alleviation of symptoms of musculardystrophy in clinical trials and animal experiments, lowering of serumurea nitrogen which is to be an indicator of modification and necrosisof muscle fiber, and lowering of concentration of creatinine in bloodwhich is a non-protein nitrogen compound produced from creatine inmuscle and an indicator of side effects of muscular dystrophy, and thelike.

A method for producing the caldecrin is not particularly limited, andthe caldecrin can be produced by a publicly known method or by animprovement method based on the publicly known method.

For example, the caldecrin can be isolated and purified from ratpancreas as a natural protein according to a method by Tomomura et. al.(refer to Tomomura et al., Journal of Biological Chemistry, 270, pp.30315-30321 (1995). The content of the document is incorporated byreference herein). In such a case, caldecrin is purified as themature-type activated by a protease existing together.

More specifically, an acetone powder is obtained by crushing a ratpancreas followed by dehydration with acetone. From the powder, aprotein is purified by repeating precipitation using acetone or ammoniumsulfate, dialysis and the like, finally column chromatography. Then, afraction containing the caldecrin alone is identified by examininglowering effect of serum calcium or amino acid sequence analysis, andthe fraction is lyophilized. As a specific method for purifying theprotein, there can be listed ion exchange chromatography, gel filtrationchromatography, electrophoresis, affinity chromatography, reverse phasechromatography, salting out, and precipitation using acetone or ammoniumsulfate, and these may be suitably used in combination.

Naturally-derived caldecrin may be derived from mammal, avian species,amphibians, reptiles, or fish, but since the caldecrin in the presentinvention is used for treating human muscular dystrophy, naturalcaldecrin is preferably derived from human.

The caldecrin can be produced as a recombinant protein by a methoddescribed in Japanese unexamined patent publication No. 4-279598, thecontents of which are incorporated by reference herein, or animprovement method based on the method.

Specifically, a gene coding the prepro-type caldecrin or the like isincorporated into an appropriate vector such as IRES-GFP vector inaccordance with a conventional method. Further, the vector istransfected to an appropriate cell, and the cell is cultured. Examplesof the cell to be used in this case include a bacteria (prokaryoticcell) such as Escherichia coli and Bacillus subtilis; an yeast such asbaker's yeast; an insect cell such as a cell derived from an ovary of acommon cutworm moth (Sf9 cell line); a cell derived from an ovary of aChinese hamster (CHO cell); a cell derived from kidney of an Africangreen monkey (COS cell); and a mammal cell such as a kidney cell of ahuman fetus (HEK 293 cell). Culture conditions such as cultivationtemperature and type of medium may be those suited for the cell which isto be used. After the culture, the protein is isolated and purified fromthe medium, the fraction containing the caldecrin alone is identified,and the fraction is subjected to lyophilizations. In such a case,caldecrin is generally obtained as pro-type.

The caldecrin used in the present invention may also be obtained bychemical synthesis in accordance with a known synthesis method ofpeptide.

Alternatively, the same amino acid sequence as that of a naturalcaldecrin derived from human or rat may be formed by deleting and/orsubstituting 1, 2 or more amino acids in the natural caldecrin derivedfrom mammal other than human or rat, or adding 1, 2 or more amino acidsthereto.

The caldecrin can be administered as the pro-type or the mature-typethereof. In case of that the pro-type caldecrin is administered, thepro-type caldecrin is activated in the living body into the mature-typeto exert the activity. Alternatively, the pro-type caldecrin may beactivated by a protease such as trypsin, and then the obtained themature-type may be administered.

The caldecrin of the present invention can alleviate muscular dystrophyby being administered at a region of muscular atrophy or a region ofloss of muscle strength. As a form of drug, injection is preferred sincecaldecrin is a protein. However, needle-free administration is desirablefor patients, and any form of drug such as oral preparation and externalpreparation may be possible due to progress of technology, and thusthere is no limitation in terms of the form of drug.

The above drugs of various forms can be produced by a conventionalmethod, and common additives may be used for preparation of variousforms of drugs as components other than caldecrin which is an activeingredient. For example, a lyophilization powder drug for injection isprepared by dissolving an effective dose of purified caldecrin in adiluent such as distilled water, physiological saline and a glucoseaqueous solution; and adding a excipient such as carboxy methylcelluloseand sodium alginate; a preservative such as benzyl alcohol, benzalkoniumchloride, and phenol; a analgesia agent such as glucose, calciumgluconate, and procaine hydrochloride; a pH adjuster such ashydrochloric acid, acetic acid, citric acid, and sodium hydroxide asnecessary; and lyophilizing in accordance with a conventional method.

A dose of the caldecrin which is the therapeutic drug for musculardystrophy according to the present invention may be suitably adjustedaccording to symptoms, severity, age and sex of a muscular dystrophypatient, and normally the dose may be approximately in a range from 0.1to 1 mg per kg of the body weight.

An administration of the caldecrin according to the present invention isto be carried out normally as a subcutaneous, intramuscular orintravenous injection in a single or multiple doses in a requiredamount, and an administration by a direct injection into the muscle maypreferably enhance the effect. As an administration method, an ampulefor injection can be directly injected subcutaneously, into the muscleor intravenously. In a case of intravenous injection, it is alsopossible to use an infusion pump for administration. Further, thetherapeutic drug for muscular dystrophy of the present invention may beadministered by mixing a given amount thereof in advance with a sugarinfusion such as a dextrose solution in a treatment for musculardystrophy, or an effective dose of the drug may be given as soleadministration into peripheral veins and the like at the same time ofthe administration of sugar infusion.

In a case of a lyophilization powder drug for injection, the powder drugis diluted in distilled water, physiological saline, Ringer solution andthe like before use, and is administered in the same manner as anampule.

Another therapeutic drug for muscular dystrophy according to the presentinvention comprises a caldecrin gene. The therapeutic drug for musculardystrophy is capable of alleviating symptoms of muscular dystrophy bytransforming cells of atrophic muscles and muscles with lowered strengthor around a diseased area so as to be able to secrete caldecrin or aprotein such as caldecrin precursor containing caldecrin.

Examples of the caldecrin gene include a caldecrin gene containing agene (SEQ ID No.3) which codes pro-type rat caldecrin and a gene (SEQ IDNo.4) which codes pro-type human caldecrin. The term, “containing” abase sequence of SEQ ID No.3 or SEQ ID No.4, means that, for example, asequence which facilitates transformation of the cells and promotesexpression of caldecrin genes may be bonded before and after the basesequence. Generally, the gene coding prepro-type caldecrin istransfected. In such a case, caldecrin is biosynthesized in cell, and isexcreted in the blood as pro-type.

The caldecrin gene can be produced by a conventional method in a generalgenetic engineering field. For example, cDNA library is first preparedfrom a cell which produces caldecrin using a conventional method such asreverse transcription of mRNA. From the cDNA library, cDNA containing acaldecrin gene is obtained using a probe or an antibody for identifyinga caldecrin gene. The cDNA is then amplified by polymerase chainreaction and further purified by a column and the like. Then, theobtained DNA may be introduced to a cell for further increasing theamount of DNA.

The caldecrin gene is preferably introduced into a vector in order totransfer the gene to a diseased area or around the diseased area as atherapeutic drug. The vector is not particularly limited as long as itis generally used for administration to human, and for example, aplasmid vector such as pCAGGS, pIRES-GFP and pIRES-bleo may be used. Thevector may be encapsulated in liposome and the like in order tofacilitate incorporation of the caldecrin gene into a targeted cell byendocytosis. Additionally, a virus vector such as adenovirus may beused.

The therapeutic drug for muscular dystrophy of the present inventioncomprises the caldecrin or the expression vector in which the genecoding the caldecrin is inserted as active ingredients, and ispreferably used together with another appropriate diluent and anadditive in an appropriate form of drug.

The administration method of the therapeutic drug for muscular dystrophycontaining the caldecrin gene according to the present invention is notparticularly limited. For example, the therapeutic drug may beadministered as an injection after being suspended in a diluent such asphysiological saline followed by further adding another additive asnecessary to be formed into an appropriate form of drug.

The dose of the therapeutic drug for muscular dystrophy containing thecaldecrin gene according to the present invention may be also suitablyadjusted according to symptoms, severity, age and sex of a musculardystrophy patient, and normally the dose may be approximately in a rangefrom 0.1 to 10 mg per kg of the body weight.

The cells transformed by the caldecrin gene according to the presentinvention secrete the caldecrin to alleviate symptoms of musculardystrophy. Therefore, cells of a patient are transformed in vitro by thecaldecrin gene of the present invention, then the transformed cells maybe transplanted in the diseased area or around the diseased area totreat muscular dystrophy.

The therapeutic drug for muscular dystrophy of the present invention hasa highly excellent effect on muscular dystrophy. Further, thetherapeutic drug does not impart any damage to renal function.Therefore, the therapeutic drug for muscular dystrophy of the presentinvention is expected to be a practical therapeutic drug for musculardystrophy for which no effective therapeutic drug is present yet.

EXAMPLES

Hereinafter, the present invention will be described in more detail withreference to Examples, but the present invention is not restricted bythe following Examples and can be suitably modified within the scopedescribed above or below, and such modifications are also included inthe technical scope of the present invention.

Production Example 1 Purification of Caldecrin from Rat Pancreas

Twenty five rats obtained from Saitama Experimental Animals Supply Co.,Ltd. were killed by administering Nembutal to take out pancreasestherefrom. The obtained pancreases were crushed by a homogenizer(Product name: Polytron manufactured by Central Scientific Commerce,Inc.), and dehydrated by adding acetone. Then, 0.1 M Tris-HCl (pH 8.0)containing 2% NaCl was added thereto, and the mixture was filtratedafter being stirred well. Cold acetone at a ratio of 0.4 by volume wasadded into the filtrate to make acetone concentration 30% by volume, andthe filtrate was stirred for 30 minutes under a condition chilled withice followed by centrifugation to give a supernatant. Further, a coldacetone at a ratio of 0.6 by volume was added to make the acetoneconcentration 60% by volume, and the mixture was stirred for 30 minutesunder a condition chilled with ice followed by precipitation bycentrifugation to give 30 to 60% acetone fraction. The obtained 30 to60% acetone fraction was dissolved in distilled water and was furtherdialyzed with distilled water to remove the acetone. Further, 45%ammonium sulfate was added thereto, and the mixture was stirred at 4° C.for 30 minutes followed by centrifugation. Ammonium sulfate was added tothe obtained supernatant so that the concentration became 60%, and themixture was stirred at 4° C. for 30 minutes followed by centrifugationto obtain 45 to 60% ammonium sulfate fraction. The 45 to 60% ammoniumsulfate fraction was dissolved in distilled water followed bylyophilization, and was kept in a dark cold place until the time of use.

The 45 to 60% ammonium sulfate fraction was dissolved in 50 mM aceticacid buffer solution (pH 5.5), and was dialyzed with the buffer solutionfollowed by purification of the solution by Q-Sepharose Fast FlowColumn, Superdex 75HR Column and Mono Q HR Column to obtain a protein.

The obtained protein was analyzed by HPLC using a reversed-phase columnand SDS-polyacrylamide gel electrophoresis, and was identified to be asingle protein. Additionally, the amino acid sequence of the protein wasanalyzed by a gas-phase sequencer, and the protein was identified ascaldecrin since the amino acid sequence of SEQ ID No.1 was present atN-terminal or the proximity of N-terminal.

The caldecrin was dissolved in phosphate buffer solution to be asolution at concentration of 1 mg/mL followed by filtration andsterilization using a filter having a pore size of 0.22 μm. The filtratewas injected into sterilized vials in an amount of 1 mL for each. Theeach filtrate in vial was subjected to vacuum lyophilization followed bybeing stopped airtight, and was kept in a dark cold place until the timeof use.

Production Example 2 Production of Pancreas Extract (PX)

In accordance with a method described in Takaoka et al., Acta MedicaNagasakiensia, vol. 13, No. 1-2, pp. 28-35, (1969), pancreas extractcontaining a plurality of elastase mixtures as main components wasprepared. More specifically, into 10 g of a commercially available pigacetone powder (manufactured by Sigma), cold water in an amount of 10times by weight ratio was added, and the mixture was subjected toextraction for 1 hour in a cold place followed by filtration. Thendiluted hydrochloric acid was added to the obtained filtrate foradjusting pH to 4 to form precipitate. The precipitate was separated bycentrifugation at 3,000 rpm for 10 minutes. The precipitate wasdissolved in water, and diluted hydrochloric acid was added to thesolution to adjust pH to 5.4. The resultant precipitate was separated bycentrifugation. Diluted hydrochloric acid was added to the obtainedsupernatant for readjusting pH to 4.0 to generate precipitate. Further,the precipitate was separated by centrifugation, and was dissolved inpurified water. Into the solution, 40% ammonium sulfate was added, andthe mixture was kept still at room temperature for 1 hour. The resultantprecipitate was separated by centrifugation. Water was added to theobtained precipitate to be dissolved, and the mixture was subjected todialysis using a dialysis tube (Cut off 3,500<) with purified water.Further, 80% ammonium sulfate was added to the dialysate to obtainprecipitate. The precipitate was dissolved again in purified waterfollowed by dialysis. The obtained purified solution was subjected tolyophilization to obtain 1.2 mg of pancreas extract. The extract wasconfirmed to be a protein by Biuret method. The obtained pancreasextract was sterilized in the same manner as in Production example 1.

Production Example 3 Production of Caldecrin Using a Gene

PCR reaction was carried out using human caldecrin cDNA (cloned fromcDNA library of Stratagene) as a template and Bsa I primer (S: SEQ IDNo.9, AS: SEQ ID No.10) as primers. More specifically, Pfu DNApolymerase available from Stratagene was used as polymerase, and a cycleof the reactions at 96° C. for 45 seconds, at 50° C. for 1 minute, andat 72° C. for 2 minutes was repeated 30 times. The amplified humancaldecrin cDNA was subjected to ligation with Bsa I site of pEXPR-IBA 3vector. The vector is one in which DNA sequence of STREP-tag is ligatedto 3′ target DNA in order to fuse a streptavidin binding tag(STREP-tagII) to C-terminal of a protein to be obtained finally. Thevector was transfected with Escherichia coli (Top 10 manufactured byInvitrogen), and the Escherichia coli was cultured in LB/Amp medium at37° C. over a night. Next, the vector DNA was purified using NucleoSpinExtract II kit manufactured by Macherey-Nagel to obtain human caldecrincDNA in which Strep-tag was fused to the C-terminal.

Using the obtained cDNA as a template, and DNA of SEQ ID No.11 as theSense primer and STREP-tag-NotI DNA of SEQ ID No.12 as the Antisenseprimer, polymerase chain reaction was carried out. More specifically,Pfu DNA polymerase available from Stratagene as polymerase was used, anda cycle of the reactions at 94° C. for 30 seconds, at 60° C. for 30seconds, and at 68° C. for 2 minutes was repeated 32 times. Theamplified human caldecrin DNA was subjected to ligation with Eco RV-NotI site of pIRES-bleo3 vector. The vector was transfected withEscherichia coli (DH5α manufactured by TAKARA) to purify DNA by the sameconditions as the above. With a use of Lipofectin Reagent, the obtainedDNA was transfected with HEK293T cell manufactured by Gibco BRL.Separately, bleomycin in an amount of 400 μg/mL was added to DMEMGlutaMAX-I medium manufactured by Gibco BRL (10% FBS, 100 μg/mLpenicillin G, 0.25 μg/mL streptomycin). In the medium, the transfectedHEK293T cells were selectively cultured at 37° C. for 14 days.

The medium was centrifuged at 700 rpm for 10 minutes, and 65% ammoniumsulfate was added to the supernatant to precipitate protein. Aftercentrifugation at 12,000 rpm for 30 minutes, the obtained precipitatewas dissolved by addition of washing buffer solution (100 mM Tris-HCl pH8, 150 mM NaCl, 1 mM EDTA). The solution was applied to Strept-Tactinimmobilized gel (Strep-Tactin Superflow column) and washed with thebuffer solution for cleaning, and then the protein was eluted by anelution buffer containing Destiobiotin, 100 mM Tris-HCl pH8, 150 mM NaCland 1 mM EDTA containing. The obtained eluate was subjected to dialysisby 20 mM Tris-HCl (pH 7.0), followed by being applied to Mono Sion-exchange column equilibrated by 20 mM Tris-HCl (pH 7.0) and elutedby 20 mM Tris-HCl (pH 7.0) containing 500 mM NaCl to give pro-type humancaldecrin which does not show protease activity. The pro-type humancaldecrin was fused with a tag at C-terminal for binding toStrept-Tactin.

Production Example 4 Preparation of Human Caldecrin Gene ExpressionVector

By the same conditions as Production example 3, PCR was carried outusing phCaldecrin-IRES-bleo as a template and Sac I-ATG caldecrin andSTREP-tag-Not I as primers to amplify human caldecrin DNA. The obtainedDNA was incorporated into Sac I-Not I site of pIRES-hrGFP. The vectorwas encapsulated in liposome of Genome One-Neo available from ISHIHARASANGYO KAISHA, LTD. Genome One-Neo is a vector containing of a membraneof hemagglutinating virus of Japan (HVJ). The vector, while retainingcell adhesion activity and completely inactivating virus proliferationactivity thereof, is incorporated to a cell together with a gene fortreatment by endocytosis. Therefore, the obtained cell incorporatinghuman caldecrin gene expression vector can express human caldecrin geneand produce caldecrin.

Test Example 1

Eight-week old C57BL/6J (dy/dy) male mice obtained from CentralInstitute for Experimental Animals were divided into three groups eachconsisting of three mice. The mice were mutant-type musculardystrophy-affected model mice, and were not able to move their lowerlimbs and feed themselves with food and water, showing an incidence ofsymptoms similar to muscular dystrophy. On a morning after fastingovernight after one week of habituation, caldecrin prepared in the samemanner as Production example 1 at a dose of 100 μg per 1 kg of the bodyweight was administered to one side of femoral muscle of mice of twogroups by intramuscular injection, while phosphate buffer solution wasadministered to a control group. After the administration, blood samplewas taken at 3 hours and 6 hours respectively to measure concentration(mg/dl) of serum urea nitrogen (hereinafter abbreviated as “BUN”occasionally) using urea nitrogen B-Test Wako kit manufactured by WakoPure Chemical Industries, Ltd. The results are shown in Table 1. Thevalues in the table are mean±standard deviation, and “Proportion” showsthe rate of BUN value of caldecrin administration group with respect tocontrol group.

TABLE 1 Caldecrin- administration Proportion Control group group (%) BUNvalue 3 hours 28.92 ± 2.08 21.02 ± 1.16 72.7 (mg/dl) after 6 hours 25.23± 1.13 20.47 ± 0.91 81.1 after

As the above results, urea nitrogen level in serum was clearly loweredto about 70 to 80% compared with the control group by the administrationof caldecrin. Since urea nitrogen level in serum increases with acollapse of muscular tissues, it has been demonstrated that caldecrincan suppress the collapse of muscular tissues.

Test Example 2

Two kinds of dymice, i.e. mutant-type (dy/dy) and wild-type, weredivided into three groups with three mice each. Separately, humancaldecrin obtained in Production example 3 was activated with trypsin inan amount of one fiftieth of the caldecrin for 30 minutes, and proteaseactivity was suppressed with 1 mM of PMSF. After habituation for 1 week,the human caldecrin was administered to a group of mice by injection ata dose of 100 μg per 1 kg of the body weight for 4 consecutive days. Tothe control group, phosphate buffer solution was administered in thesame manner. These groups fasted overnight before a last administration,and they were killed 3 hours after the last administration to collectblood sample on the following day.

To the remaining one group, a solution of 10 μg of DNA/100 μL preparedfrom human caldecrin gene expression vector of Production example 4 wasadministered by intramuscular injection to one side of femoral muscle ata dose of 100 μL per mouse. Since it takes at least one day from theadministration of DNA to the expression of protein, mice were killedafter five days from the administration. The mice fasted one day beforebeing killed, and blood sample was taken after the mice were killed.

Serum was separated from blood samples taken from each group todetermine BUN concentration (mg/dl). The results are shown in FIG. 1. Asshown in FIG. 1, in both mutant-type and wild-type dy mice, BUN level inserum could be lowered by administration of caldecrin.

Test Example 3

In the same manner as Test example 2, after mutant-type dy/dy mice werehabituated for 1 week while normal mice of a same kind were used as acontrol group, human caldecrin of Production example 3 and humancaldecrin gene transfection liposome of Production example 4 wereadministered. The human caldecrin was administered by intraperitonealinjection at a dose of 100 μg per 1 kg of the body weight for 4consecutive days, and the mice were killed 3 hours after the lastadministration. The human caldecrin gene transfection liposome wasinjected to one side of femoral muscle at a dose of 100 μL (including 10μg of DNA) in a state of solution per one mouse and the mice were killedafter 5 days. To the control group, phosphate buffer solution wasadministered by the same conditions as the administration of humancaldecrin. Each group fasted a day before being killed.

To each group, 1% Evans blue (EV) dissolved in PBS was administered byinjection 24 hours before the mice were killed at a dose of 50 μL per 10g of the body weight. The Evans blue does not penetrate into anundamaged cell, but when a cell membrane is damaged, the Evans bluepenetrates into the cell. After mice were killed, femoral muscle wastaken out and a part of it was fixed with 10% formalin while anotherpart thereof was frozen. In the group administered human caldecrin genetransfection liposome, the femoral muscle was taken out from an oppositeside of the leg which was subjected to intramuscular injection.

From formalin-fixed muscle, a slice of the femoral muscle at a maximumcross-section was obtained to be subjected to HE stain. Results areshown in FIG. 2. As in FIG. 2, muscular tissue of a normal mouse hadless irregularity of cross-section of muscle fiber, and a dark-colorednucleus was found around the muscle fiber. However, in muscular tissueof the control group of the muscular dystrophy-affected model mouse, dueto modification and necrosis of muscle fiber, muscle fibers which werethinner, in other words, having smaller area of cross-section wereformed, and nucleuses were transferred around a center of the musclefiber. On the other hand, in a mouse administered caldecrin and acaldecrin gene, a basic structure of the muscular tissue was wellmaintained, and symptoms were clearly improved.

From frozen femoral muscle, a frozen section of 10 μm was prepared andautonomous fluorescence by Evans blue was observed using fluorescentmicroscope. Photographs of the fluorescent microscope are shown in FIG.3. As shown in FIG. 3, when the images of the tissue were observed usingfluorescent microscope, red fluorescent caused by Evans blueadministered one day before killing was localized around the musclefiber because muscular tissue was well maintained in a normal mouse.Evans blue was specifically incorporated into collapsed muscle fiber tostain the fiber. Therefore, the results show that there was no damage innormal mouse since almost no Evans blue was present in muscular cell.The same can be said for mice administered caldecrin or transfected withcaldecrin gene. On the other hand, in muscular tissue of musculardystrophy-affected model mouse, an irregularity of area of cross-sectionof muscle fiber due to modification and necrosis of muscle fiber wasobserved, and Evans blue penetrated into the muscle fiber. In contrast,in muscular tissue administered caldecrin or a caldecrin gene, the ratioof red fluorescent image was clearly decreased though intrusion of Evansblue into a part of muscle fiber was observed, demonstrating an effectof caldecrin and caldecrin gene on suppressing collapse of musculartissue.

Test Example 4

Six-week old BALB/cCr Slc male mice fasted from one day before the test.Separately, the human caldecrin obtained in Production example 3 or thepig pancreas extract obtained in Production example 2 was dissolved inphosphate buffer solution to prepare a solution of a concentration of0.01 mg/mL. The mice were divided into groups having 4 or 5 mice each,and were intraperitoneally-injected with a phosphate buffer solutionalone, a human caldecrin solution, or a pancreas extract solution at adose of 0.1 mL per 10 g of the body weight. Five hours after theadministration, blood sample was taken from the heart, and serum ureanitrogen level (mg/dl) and creatinine level (mg/dl) were determinedusing BUN Test Wako and creatinine Test Wako kit. The result of theserum urea nitrogen level is shown in Table 2 while the result ofcreatinine level is shown in Table 3.

TABLE 2 BUN (mg/dl) ± Number standard Proportion of mice deviationt-TEST (%) Control group 4 26.6 ± 3.00 100 Caldecrin- 5 22.3 ± 1.640.0142 83.8 administration Group PX- 4 25.4 ± 4.08 0.318 95.5administration group

TABLE 3 Creatinine (mg/dl) ± standard Proportion BUN/ deviation t-TEST(%) creatinine Control group 1.44 ± 0.00297 100 18.5 Caldecrin- 1.53 ±0.1 0.123 106.3 14.6 administration Group PX- 1.95 ± 0.0016 9.63 × 10⁻⁵135 13.0 administration group

As in the above results, although serum urea nitrogen level could belowered by an administration of pancreas extract, the level was furtherlowered compared with the case of the administration of caldecrin.Therefore, it has been demonstrated that caldecrin can suppress thecollapse of muscular tissue caused by muscular dystrophy moreeffectively.

Further, creatinine level in blood was rather increased by pancreasextract. The creatinine is basically supposed to be discharged intourine via kidney, so that the creatinine level in blood is used forevaluating renal function. Therefore, the results strongly suggest thatthe renal function was damaged by administration of pancreas extract.

On the other hand, when caldecrin was administered, an increase in thecreatinine level in blood was markedly suppressed, and the level wasalmost the same as the control group. This fact suggests that musculardystrophy can be treated by the administration of caldecrin withoutaffecting adversely on renal function.

As described above, although caldecrin is a protein derived frompancreas and having a DNA sequence similar to elastase, caldecrin hasmuch higher decreasing-effect on serum urea nitrogen than PX which is acrude extract of pancreas including elastase mixture as a maincomponent. While PX has a possibility of affecting adversely on renalfunction since PX increases creatinine level in blood, caldecrin doesnot have such a defect. Therefore, caldecrin and a gene thereof areextremely effective as agents for treating muscular dystrophy for whichno effective therapeutic agent exists.

1. A muscular dystrophy drug, comprising a caldecrin.
 2. A musculardystrophy drug, comprising a following protein (a) or a followingprotein (b): (a) a protein having amino acid sequence of SEQ ID No. 1 orSEQ ID No. 2; (b) a protein formed by deletion, substitution and/oraddition of one or several amino acids of a protein having the aminoacid sequence of SEQ ID No. 1 or SEQ ID No. 2, and having therapeuticeffect on muscular dystrophy.
 3. A muscular dystrophy drug, comprising acaldecrin gene.
 4. A muscular dystrophy drug, comprising a caldecringene having a base sequence of SEQ ID No. 3 or SEQ ID No.
 4. 5. Avector, comprising the caldecrin gene according to claim
 3. 6. A vector,comprising the caldecrin gene according to claim
 4. 7. A transformedcell, comprising the vector according to claim
 5. 8. A transformed cell,comprising the vector according to claim 6.